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TR200101245T2 - N-arylsulfonyl-amino-omega-amides - Google Patents

N-arylsulfonyl-amino-omega-amides

Info

Publication number
TR200101245T2
TR200101245T2 TR2001/01245T TR200101245T TR200101245T2 TR 200101245 T2 TR200101245 T2 TR 200101245T2 TR 2001/01245 T TR2001/01245 T TR 2001/01245T TR 200101245 T TR200101245 T TR 200101245T TR 200101245 T2 TR200101245 T2 TR 200101245T2
Authority
TR
Turkey
Prior art keywords
arylsulfonyl
omega
amides
amino
formula
Prior art date
Application number
TR2001/01245T
Other languages
Turkish (tr)
Inventor
Schwab Wilfried
Thorwart Werner
Schudok Manfred
Haase Burkhard
Original Assignee
Aventis Pharma Deutschland Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aventis Pharma Deutschland Gmbh filed Critical Aventis Pharma Deutschland Gmbh
Publication of TR200101245T2 publication Critical patent/TR200101245T2/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/19—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Indole Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

Formül I bilesikleri ve/veya formül I bilesiginin bir stereoizomer hali ve/veya formül I bilesiginin fizyolojik olarak tolere edilebilir tuzu, matris parçalayici metaloproteinazlarin etkili oldugu hastaliklarin tedavisine ve hastaliklarin önlenmesine yönelik tibbi ilaçlarin üretimine uygunluk göstermektedirler.The compounds of formula I and / or a stereoisomer form of the compound of formula I and / or the physiologically tolerable salt of the compound of formula I are suitable for the treatment of diseases in which matrix disintegrating metalloproteinases are effective and for the production of medical drugs for the prevention of diseases.

TR2001/01245T 1998-11-06 1999-10-21 N-arylsulfonyl-amino-omega-amides TR200101245T2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19851184A DE19851184A1 (en) 1998-11-06 1998-11-06 N-arylsulfonylamino acid omega amides

Publications (1)

Publication Number Publication Date
TR200101245T2 true TR200101245T2 (en) 2001-10-22

Family

ID=7886902

Family Applications (1)

Application Number Title Priority Date Filing Date
TR2001/01245T TR200101245T2 (en) 1998-11-06 1999-10-21 N-arylsulfonyl-amino-omega-amides

Country Status (23)

Country Link
US (2) US6201130B1 (en)
EP (1) EP1124797B1 (en)
JP (1) JP4348014B2 (en)
KR (1) KR100655632B1 (en)
CN (1) CN1206213C (en)
AR (1) AR021086A1 (en)
AT (1) ATE260889T1 (en)
AU (1) AU757602B2 (en)
BR (1) BR9915729A (en)
CA (1) CA2350031C (en)
CZ (1) CZ302291B6 (en)
DE (2) DE19851184A1 (en)
DK (1) DK1124797T3 (en)
ES (1) ES2213405T3 (en)
HK (1) HK1041686B (en)
HU (1) HUP0104122A3 (en)
ID (1) ID28810A (en)
PL (1) PL198827B1 (en)
PT (1) PT1124797E (en)
RU (1) RU2228330C2 (en)
TR (1) TR200101245T2 (en)
WO (1) WO2000027808A1 (en)
ZA (1) ZA200103485B (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PA8557501A1 (en) 2001-11-12 2003-06-30 Pfizer Prod Inc BENZAMIDA, HETEROARILAMIDA AND INVESTED AMIDAS
WO2003042190A1 (en) 2001-11-12 2003-05-22 Pfizer Products Inc. N-alkyl-adamantyl derivatives as p2x7-receptor antagonists
PA8591801A1 (en) 2002-12-31 2004-07-26 Pfizer Prod Inc BENZAMID INHIBITORS OF THE P2X7 RECEIVER.
US7071223B1 (en) * 2002-12-31 2006-07-04 Pfizer, Inc. Benzamide inhibitors of the P2X7 receptor
MXPA05010165A (en) * 2003-04-15 2005-11-16 Warner Lambert Co [c]-fused bicyclic proline derivatives and their use for treating arthritic conditions.
BRPI0410349A (en) * 2003-05-12 2006-05-30 Pfizer Prod Inc p2x7 receptor benzamide inhibitors
KR20070115583A (en) * 2004-06-29 2007-12-06 화이자 프로덕츠 인코포레이티드 Method for preparing 5-[4-(2-hydroxy-ehtyl)-3,5-dioxo-4,5-dihydro-3h-[1,2,4]-triazin-2-yl]-benzamide derivatives with p2x7 inhibiting activity by reaction of the derivative unsubstituted in 4-position of the triazine with an oxiran in the presence of a lewis acid
RU2006146675A (en) * 2004-06-29 2008-07-10 Пфайзер Продактс Инк. (Us) METHOD FOR PRODUCING 5- [4- (2-HYDROXYPROPYL) -3,5-DIOXO-4,5-DIHYDRO-3H- [1,2,4] TRIAZIN-2-IL] BENZAMIDE DERIVATIVES BY REMOVING PROTECTION FROM INTERMEDIATE PRODUCTS, SODA HYDROXYL
CA2572119A1 (en) * 2004-06-29 2006-01-12 Warner-Lambert Company Llc Combination therapies utilizing benzamide inhibitors of the p2x7 receptor
US7576222B2 (en) 2004-12-28 2009-08-18 Wyeth Alkynyl-containing tryptophan derivative inhibitors of TACE/matrix metalloproteinase
TW200800209A (en) 2005-07-11 2008-01-01 Wyeth Corp Glutamate aggrecanase inhibitors
PE20070526A1 (en) 2005-10-13 2007-06-11 Wyeth Corp METHODS FOR PREPARING GLUTAMIC ACID DERIVATIVES
ES2533065T3 (en) 2010-07-09 2015-04-07 Pfizer Limited Benzenesulfonamides useful as sodium channel inhibitors
CA2900116C (en) * 2013-02-06 2021-08-10 Merck Patent Gmbh Substituted carboxylic acid derivatives as aggrecanase inhibitors for the treatment of osteoarthritis

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU1063026A1 (en) * 1982-05-19 1990-12-07 Институт биохимии АН ЛитССР N-benzosulphonyl derivatives of treo-dl-phenylserine as antiinflammatory agent
JP2764262B2 (en) 1987-08-28 1998-06-11 持田製薬株式会社 Hydantoin derivative and pharmaceutical composition containing the same as active ingredient
TW201303B (en) 1990-07-05 1993-03-01 Hoffmann La Roche
US5455258A (en) * 1993-01-06 1995-10-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
GB2303629B (en) 1994-06-22 1998-09-02 British Biotech Pharm Hydroxamic acids and their use as metalloproteinase inhibitors
US5863949A (en) * 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
WO1997001599A1 (en) * 1995-06-28 1997-01-16 E.I. Du Pont De Nemours And Company Fluoropolymer nanocomposites
KR980009238A (en) 1995-07-28 1998-04-30 우에노 도시오 Sulfonyl amino acid derivative
NZ332711A (en) * 1996-05-17 2000-06-23 Warner Lambert Co Biphenylsulfonylamino carboxylic acid derivatives as matrix metalloproteinase inhibitors
DE19719621A1 (en) * 1997-05-09 1998-11-12 Hoechst Ag Sulfonylaminocarboxylic acids

Also Published As

Publication number Publication date
CZ302291B6 (en) 2011-02-09
PL347574A1 (en) 2002-04-08
BR9915729A (en) 2001-10-23
PL198827B1 (en) 2008-07-31
JP2002529447A (en) 2002-09-10
PT1124797E (en) 2004-07-30
AU1153000A (en) 2000-05-29
RU2228330C2 (en) 2004-05-10
US6201130B1 (en) 2001-03-13
EP1124797A1 (en) 2001-08-22
ATE260889T1 (en) 2004-03-15
HUP0104122A2 (en) 2002-03-28
AR021086A1 (en) 2002-06-12
ES2213405T3 (en) 2004-08-16
ID28810A (en) 2001-07-05
HUP0104122A3 (en) 2002-04-29
US6335333B1 (en) 2002-01-01
KR100655632B1 (en) 2006-12-12
JP4348014B2 (en) 2009-10-21
CZ20011506A3 (en) 2001-08-15
WO2000027808A1 (en) 2000-05-18
CN1332724A (en) 2002-01-23
HK1041686A1 (en) 2002-07-19
AU757602B2 (en) 2003-02-27
KR20010080385A (en) 2001-08-22
CA2350031A1 (en) 2000-05-18
ZA200103485B (en) 2001-12-04
EP1124797B1 (en) 2004-03-03
DE19851184A1 (en) 2000-05-11
HK1041686B (en) 2005-09-23
CN1206213C (en) 2005-06-15
DK1124797T3 (en) 2004-07-05
CA2350031C (en) 2010-01-26
DE59908769D1 (en) 2004-04-08

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